Abstract

Understanding the relationships among biomolecules and how these relationships change between healthy and disease states is an important question in modern biology and medicine. The advances in high-throughput techniques has led to the explosion of biological data available for analysis, allowing researchers to investigate multiple molecular layers (i.e. omics data) together. The classical statistical methods could not address the challenges of combining multiple data types, leading to the development of ad hoc methodologies, which however depend on several factors. Among those, it is important to consider whether “prior knowledge” on the inter-omics relationships is available for integration. To address this issue, we thus focused on different approaches to perform three-omics integration: supervised (prior knowledge is available), unsupervised and semi-supervised. With the supervised integration of DNA methylation, gene expression and protein levels from adipocytes we observed coordinated significant changes across the three omics in the last phase of adipogenesis. However, in most cases, interactions between different molecular layers are complex and unknown: we explored unsupervised integration methods, showing that their results are influenced by method choice, pre-processing, number of integrated data types and experimental design. The strength of the inter-omics signal and the presence of noise are also proven as relevant factors. Since the inclusion of prior knowledge can highlight the former while decreasing the influence of the latter, we proposed a semi-supervised approach, showing that the inclusion of knowledge about inter-omics interactions increases the accuracy of unsupervised methods when solving the problem of sample classification.